Associated Papers
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.
Merz LM et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2025
Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia.
Chen L et al.
Translational Psychiatry, 2024
38951484 (PubMed )
Supplement: 41398_2024_2984_MOESM1_ESM.pdf
Dysregulation of neuron differentiation in an autistic savant with exceptional memory.
Song J et al.
Molecular Brain, 2019
31699123 (PubMed )
Supplement: 13041_2019_507_MOESM1_ESM.xlsx › SNPs_merged_1000g_deleterious
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